It was a horrible diagnosis, but looking back, Pamela Marshall is thankful her son Ethan...
The Tulsa-based Global Foundation for Peroxisomal Disorders has named Melissa Bryce Gamble as its first...
Dr. Braverman’s work focuses on genes responsible for the proper function of peroxisomes, which are...
Gideon Jolicoeur, 4, was born with a rare condition that impacts his hearing and eyesight...
Jaxon’s health has had a backslide lately. The hospice nurses hope he will make it...
De Jesus says that it was a specialist in Canada who diagnosed Jaxson with Peroxisomal...
She's five-years-old, loves all things pink and glitter, and will be sporting a pretty magical...
Thomas Thériault, of Saint-Quentin, will celebrate his second birthday on November 24. His community recently...
The Jersey County Journal featured a letter to the editor, from Vicky Maag, about our...
Melissa Bryce Gamble is president and co-founder of the Global Foundation for Peroxisomal Disorders, which...
